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Brief Title: A Study Of Sunitinib Compared To Placebo For Patients With Advanced Pancreatic Islet Cell Tumors
Official Title: A Phase III Randomized, Double-Blind Study Of Sunitinib (SU011248, SUTENT) Versus Placebo In Patients With Progressive Advanced/Metastatic Well-Differentiated Pancreatic Islet Cell Tumors
Study ID: NCT00428597
Brief Summary: This study randomized patients with advanced pancreatic islet cell tumors to receive either sunitinib or placebo. Patients who were randomized to sunitinib received 37.5 mg of sunitinib daily, those randomized to placebo received a tablet that looked similar but had no active drug. Neither the patient or the doctor knew whether the patient was receiving sunitinib or placebo. Patients were followed to determine the status and size of their tumors, survival, quality of life and safety of the drug. The study was designed to detect a 50% improvement in median PFS\[Progression Free Survival\] with 90% power and was to enroll 340 subjects. An interim analysis was planned when 130 events had occurred, and the final analysis was to be conducted when 260 events had occurred. Study A6181111 was stopped early during the enrollment period because of a clear and clinically meaningful improvement in efficacy for the sunitinib treatment arm as recommended by the DMC \[Data Monitoring Committee\]. The actual number of subjects enrolled was 171 and the actual number of PFS events recorded was 81 PFS events. The decision to terminate the study was not based on safety concerns related to sunitinib administration.
Detailed Description: The study was terminated on 11 March 2009 because the independent Data Monitoring Committee determined that the study had met its primary endpoint in demonstrating improvement in progression-free survival. The decision to terminate the trial was not based on safety concerns related to sunitinib administration.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Pfizer Investigational Site, Aurora, Colorado, United States
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Pfizer Investigational Site, Worcester, Massachusetts, United States
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Pfizer Investigational Site, Austin, Texas, United States
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Pfizer Investigational Site, Perth, Western Australia, Australia
Pfizer Investigational Site, Bruxelles, , Belgium
Pfizer Investigational Site, Bruxelles, , Belgium
Pfizer Investigational Site, Leuven, , Belgium
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Pfizer Investigational Site, Halifax, Nova Scotia, Canada
Pfizer Investigational Site, Halifax, Nova Scotia, Canada
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Pfizer Investigational Site, Montreal, Quebec, Canada
Pfizer Investigational Site, Montreal, Quebec, Canada
Pfizer Investigational Site, Paris, Be1 05677, France
Pfizer Investigational Site, Paris, Cedex, France
Pfizer Investigational Site, Bordeaux, , France
Pfizer Investigational Site, Clichy Cedex, , France
Pfizer Investigational Site, Lyon, , France
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Pfizer Investigational Site, Bad Berka, , Germany
Pfizer Investigational Site, Berlin, , Germany
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Pfizer Investigational Site, Luebeck, , Germany
Pfizer Investigational Site, Marburg, , Germany
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Pfizer Investigational Site, Cremona, , Italy
Pfizer Investigational Site, Milano, , Italy
Pfizer Investigational Site, Rozzano (MI), , Italy
Pfizer Investigational Site, Seoul, , Korea, Republic of
Pfizer Investigational Site, Seoul, , Korea, Republic of
Pfizer Investigational Site, Barcelona, , Spain
Pfizer Investigational Site, Barcelona, , Spain
Pfizer Investigational Site, Madrid, , Spain
Pfizer Investigational Site, Madrid, , Spain
Pfizer Investigational Site, Madrid, , Spain
Pfizer Investigational Site, Kwei-Shan, Taoyuan, Taiwan
Pfizer Investigational Site, Taipei, , Taiwan
Pfizer Investigational Site, Leeds, , United Kingdom
Pfizer Investigational Site, Liverpool, , United Kingdom
Pfizer Investigational Site, Manchester, , United Kingdom
Name: Pfizer CT.gov Call Center
Affiliation: Pfizer
Role: STUDY_DIRECTOR